D. Bouron‐Dal Soglio

发表

Extending the phenotypes associated with DICER1 mutations

W. Foulkes, N. Hamel, B. Pasini, 2011, Human mutation.

A child with neuroblastoma and metachronous anaplastic sarcoma of the kidney: Underlying DICER1 syndrome?

R. Siebert, W. Foulkes, E. Perlman, 2020, Pediatric blood & cancer.

Novel PDE10A-BRAF Fusion With Concomitant NF1 Mutation Identified in an Undifferentiated Sarcoma of Infancy With Sustained Response to Trametinib.

P. Gendron, E. Lemyre, C. Kleinman, 2018, JCO precision oncology.

High-sensitivity sequencing reveals multi-organ somatic mosaicism causing DICER1 syndrome

J. Ragoussis, W. Foulkes, S. Hopman, 2015, Journal of Medical Genetics.

A Case Report of Syndromic Multinodular Goitre in Adolescence: Exploring the Phenotype Overlap between Cowden and DICER1 Syndromes

W. Foulkes, N. Pachter, J. Walsh, 2017, European Thyroid Journal.

DICER1 mutations in familial multinodular goiter with and without ovarian Sertoli-Leydig cell tumors.

W. Foulkes, P. Broderick, R. Houlston, 2011, JAMA.

A case of neuroblastoma in DICER1 syndrome: Chance finding or noncanonical causation?

W. Foulkes, D. Bouron‐Dal Soglio, N. Sabbaghian, 2018, Pediatric blood & cancer.

Assessment of correlation between p16INK4a staining, specific subtype of human papillomavirus, and progression of LSIL/CIN1 lesions: first comparative study.

D. Bouron‐Dal Soglio, T. Ducruet, L. Oligny, 2014, American journal of clinical pathology.

A Novel PGM3 Mutation Is Associated With a Severe Phenotype of Bone Marrow Failure, Severe Combined Immunodeficiency, Skeletal Dysplasia, and Congenital Malformations

E. Haddad, V. Désilets, Philippe M. Campeau, 2017, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Germ-line and somatic DICER1 mutations in pineoblastoma

J. Lupski, S. Jhangiani, W. Foulkes, 2014, Acta Neuropathologica.

Pandemic stress and SARS-CoV-2 infection are associated with pathological changes at the maternal-fetal interface

K. Widdows, D. Bouron‐Dal Soglio, M. Sharps, 2021, Placenta.

Likely foregut endoderm origin for a postzygotic mutation affecting the RNase IIIb domain of DICER1

W. Foulkes, D. Bouron‐Dal Soglio, J. Priest, 2021, Journal of Medical Genetics.

Ovarian embryonal rhabdomyosarcoma is a rare manifestation of the DICER1 syndrome.

W. Foulkes, N. Hamel, D. Malkin, 2015, Human pathology.

Ovarian embryonal rhabdomyosarcoma is a rare manifestation of the DICER1 syndrome

W. Foulkes, N. Hamel, D. Malkin, 2014, bioRxiv.

Intestinal congenital/infantile fibrosarcoma: a new clinico-pathological entity?

M. Peuchmaur, D. Bouron‐Dal Soglio, P. Fréneaux, 2015, Pediatric Surgery International.

An immunohistochemical evaluation of C4d deposition in pediatric inflammatory liver diseases.

F. Alvarez, A. Rougemont, D. Bouron‐Dal Soglio, 2008, Human pathology.

Pituitary blastoma: a pathognomonic feature of germ-line DICER1 mutations

P. Maeder, W. Foulkes, J. Warner, 2014, Acta Neuropathologica.

Caudal dysgenesis, sirenomelia, and situs inversus totalis: A primitive defect in blastogenesis

V. Désilets, A. Rougemont, D. Bouron‐Dal Soglio, 2008, American journal of medical genetics. Part A.

Germline DICER1 mutations and familial cystic nephroma

Gretchen M. Williams, W. Foulkes, N. Hamel, 2010, Journal of Medical Genetics.

Endoscopic assessment of children with esophageal atresia: Lack of relationship of esophagitis and esophageal metaplasia to symptomatology.

C. Faure, D. Bouron‐Dal Soglio, J. Castilloux, 2010, Canadian journal of gastroenterology = Journal canadien de gastroenterologie.

SNP genotyping of a sclerosing rhabdomyosarcoma: reveals highly aneuploid profile and a specific MDM2/HMGA2 amplification.

A. Montpetit, A. Rougemont, D. Bouron‐Dal Soglio, 2009, Human pathology.

Mesenchymal Hamartoma of the Liver and DICER1 Syndrome

R. Siebert, M. Segni, W. Foulkes, 2019, The New England journal of medicine.

Implication of unfavorable histology, MYCN amplification and diploidy for stage I and II neuroblastomas.

A. Rougemont, D. Bouron‐Dal Soglio, A. S. de Buys Roessingh, 2008, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Sequencing of DICER1 in sarcomas identifies biallelic somatic DICER1 mutations in an adult-onset embryonal rhabdomyosarcoma

J. Ragoussis, P. V. van Diest, W. Foulkes, 2017, British Journal of Cancer.

A t(17;22)(q21;q12) with partial ETV4 deletion in a soft tissue Ewing sarcoma.

A. Rougemont, D. Bouron‐Dal Soglio, J. Fournet, 2012, Cancer genetics.

Mesenchymal Hamartoma of the Liver and DICER1 Syndrome. Reply.

W. Foulkes, D. Bouron‐Dal Soglio, V. Nguyen, 2019, The New England journal of medicine.

Pulmonary arteriovenous malformation mimicking congenital cystic adenomatoid malformation in a newborn.

D. Bouron‐Dal Soglio, S. Bouchard, A. Bütter, 2006, Journal of pediatric surgery.

Chondroid Cystic Malformation of the Lung With Trisomy 8 Mosaicism: A New Cystic Lung Malformation

A. Montpetit, A. Rougemont, D. Bouron‐Dal Soglio, 2008, The American journal of surgical pathology.

Multiple DICER1‐related tumors in a child with a large interstitial 14q32 deletion

S. Bens, R. Siebert, W. Foulkes, 2018, Genes, chromosomes & cancer.

Characterization of the Transition Zone in Short Segment Hirschsprung Disease Using Calretinin Immunostaining

C. Faure, D. Bouron‐Dal Soglio, L. Hart, 2021, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Male pseudohermaphroditism and gonadal mosaicism in a 47,XY,+22 fetus

E. Lemyre, D. Bouron‐Dal Soglio, J. Fournet, 2006, American journal of medical genetics. Part A.

Ossifying renal tumor of infancy: report of a case with positive WT-1 immunohistochemistry and high mitotic index and review of the literature.

D. Bouron‐Dal Soglio, L. Oligny, J. Déry, 2016, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Gray Zone Lymphoma Arising in the Neck of a Teenager With a Germline Mutation in TP53.

T. Petrella, D. Bouron‐Dal Soglio, S. Turpin, 2019, Journal of pediatric hematology/oncology.

Malignant Rhabdoid Tumor of Soft Tissue

C. Laverdière, D. Bouron‐Dal Soglio, D. Trudel, 2017, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

SNP genotyping of a sclerosing rhabdomyosarcoma: reveals highly aneuploid profile and a specific MDM2/HMGA2 amplification.

A. Montpetit, A. Rougemont, D. Bouron‐Dal Soglio, 2009, Human pathology.